Canonical Allele Identifier: CA366242159

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375027
• MyVariant Identifiers: chr6:g.157522302C>G (hg19) ; chr6:g.157201168C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201168C>G , CM000668.2:g.157201168C>G	GRCh38
NC_000006.11:g.157522302C>G , CM000668.1:g.157522302C>G	GRCh37
NC_000006.10:g.157563994C>G	NCBI36
NG_032093.1:g.428239C>G
NG_032093.2:g.428239C>G
NG_066624.1:g.430143C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4784C>G	ENSP00000055163.8:p.Ser1595Cys
ENST00000414678.8:c.4853C>G	ENSP00000412835.3:p.Ser1618Cys
ENST00000637015.2:c.5072C>G	ENSP00000489729.2:p.Ser1691Cys
ENST00000346085.10:c.4823C>G	ENSP00000344546.5:p.Ser1608Cys
ENST00000350026.10:c.4535C>G	ENSP00000055163.7:p.Ser1512Cys
ENST00000414678.7:c.3101C>G	ENSP00000412835.2:p.Ser1034Cys
ENST00000635849.1:c.2264C>G	ENSP00000490948.1:p.Ser755Cys
ENST00000635957.1:c.1895C>G	ENSP00000490385.1:p.Ser632Cys
ENST00000636227.1:n.3406C>G
ENST00000636254.1:n.863C>G
ENST00000636930.2:c.4943C>G MANE Select	ENSP00000490491.2:p.Ser1648Cys
ENST00000636940.1:n.2940C>G
ENST00000637015.1:c.2311C>G
ENST00000637568.1:c.2225C>G
ENST00000637741.1:n.1609C>G
ENST00000637810.1:c.2285C>G	ENSP00000489636.1:p.Ser762Cys
ENST00000637904.1:c.2444C>G	ENSP00000490550.1:p.Ser815Cys
ENST00000647938.1:c.4574C>G	ENSP00000498155.1:p.Ser1525Cys
ENST00000346085.9:c.4574C>G	ENSP00000344546.4:p.Ser1525Cys
ENST00000350026.9:c.4535C>G	ENSP00000055163.7:p.Ser1512Cys
ENST00000414678.6:c.3101C>G	ENSP00000412835.2:p.Ser1034Cys
NM_017519.2:c.4535C>G	NP_059989.2:p.Ser1512Cys
NM_020732.3:c.4574C>G	NP_065783.3:p.Ser1525Cys
XM_005267069.3:c.4694C>G	XP_005267126.2:p.Ser1565Cys
XM_011535984.1:c.3773C>G	XP_011534286.1:p.Ser1258Cys
XM_011535985.1:c.3593C>G	XP_011534287.1:p.Ser1198Cys
XM_011535986.1:c.3353C>G	XP_011534288.1:p.Ser1118Cys
XM_011535987.1:c.2972C>G	XP_011534289.1:p.Ser991Cys
XM_011535988.1:c.1835C>G	XP_011534290.1:p.Ser612Cys
NM_001346813.1:c.4694C>G	NP_001333742.1:p.Ser1565Cys
NM_001363725.1:c.2444C>G	NP_001350654.1:p.Ser815Cys
XM_011535984.2:c.4904C>G	XP_011534286.2:p.Ser1635Cys
XM_011535988.3:c.1835C>G	XP_011534290.1:p.Ser612Cys
XM_017011103.2:c.4805C>G	XP_016866592.1:p.Ser1602Cys
XM_017011104.1:c.4775C>G	XP_016866593.1:p.Ser1592Cys
XM_017011105.2:c.4745C>G	XP_016866594.1:p.Ser1582Cys
XM_017011106.2:c.4616C>G	XP_016866595.1:p.Ser1539Cys
XM_017011107.2:c.4595C>G	XP_016866596.1:p.Ser1532Cys
XR_002956289.1:n.4890C>G
NM_001363725.2:c.2444C>G	NP_001350654.1:p.Ser815Cys
NM_001371656.1:c.4823C>G	NP_001358585.1:p.Ser1608Cys
NM_001374820.1:c.4823C>G	NP_001361749.1:p.Ser1608Cys
NM_001374828.1:c.4943C>G MANE Select	NP_001361757.1:p.Ser1648Cys
NM_017519.3:c.4784C>G	NP_059989.3:p.Ser1595Cys